Disease association ontology term - MONDO:0014769 - inherited oocyte maturation defect

Term summary

ID: MONDO:0014769
Name: inherited oocyte maturation defect
Ontology or CV name: Disease association

Parents

is_a hereditary disease
is_a infertility disorder

Annotation

Disease association

MONDO:0030925 - oocyte maturation defect 10

References:

PB_REF:0000006

Genes:

rec7 (SPCC1753.03c)

MONDO:0859330 - oocyte maturation defect 13

References:

PB_REF:0000006

Genes:

zfs1 (SPBC1718.07c)

MONDO:0859521 - oocyte maturation defect 14

References:

PB_REF:0000006

Genes:

slp1 (SPAC821.08c)

MONDO:0021573 - oocyte maturation defect 2

References:

PB_REF:0000006

Genes:

nda3 (SPBC26H8.07c)

MONDO:0020837 - oocyte maturation defect 5

References:

PB_REF:0000006

Genes:

MONDO:0957961 - oocyte/zygote/embryo maturation arrest 21

References:

PB_REF:0000006

Genes:

chk1 (SPCC1259.13)

MONDO:0979231 - oocyte/zygote/embryo maturation arrest 23

References:

PB_REF:0000006

Genes:

MONDO:0979232 - oocyte/zygote/embryo maturation arrest 24

References:

PB_REF:0000006

Genes: